A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892696



Internal ID19183516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:54786525..54980798hg38UCSC Ensembl
Outerchr15:54786525..54980798hg38UCSC Ensembl
Innerchr15:55078723..55272996hg19UCSC Ensembl
Outerchr15:55078723..55272996hg19UCSC Ensembl
Innerchr15:52866015..53060288hg18UCSC Ensembl
Outerchr15:52866015..53060288hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38194274
hg19194274
hg18194274
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784511
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892696
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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